SAPrIm 2.0: a semi-automated protocol for mid-throughput soluble HLA immunopeptidomics

Human leukocyte antigen (HLA) molecules are pivotal in guiding human adaptive immune responses through their presentation of peptide ligands, collectively known as the immunopeptidome. This process is central to the development of cancer immunotherapies, such as vaccines and T-cell therapies. Profiling the immunopeptidome from plasma and other biofluids has gained increasing traction, as it offers a minimally invasive approach for monitoring disease states and immune responses toward cancer therapy. Here we present the second iteration of SAPrIm, a refined immunopeptidomics tool optimized for soluble HLA analysis. It can process up to 12 samples per batch within a day. In this plasma-focused iteration, we identified approximately 1,200 to 4,000 immunopeptides from 100 µL to 1 mL of plasma, demonstrating high reproducibility across technical replicates, biological replicates, and inter-day analyses. This robust reproducibility highlights the method's strong potential for reliable relative quantification of immunopeptides in plasma-based studies. This workflow is positioned to advance the field of immunopeptidomics by enabling efficient plasma-based comparative analyses and mid-size cohort studies.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-04-24
DOI
https://doi.org/10.3389/fimmu.2025.1546629
Citations
1
Primary Topic
vaccines and immunoinformatics approaches
Type
article
Field-Weighted Citation Impact
0.81
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article

SAPrIm 2.0: a semi-automated protocol for mid-throughput soluble HLA immunopeptidomics

Joshua D. Ooi, Terry C.C. Lim Kam Sian, Isaac B. Woodhouse, Joel R. Steele et al.
1 citations
Frontiers in Immunology
vaccines and immunoinformatics approaches
0.81
article

SAPrIm 2.0: a semi-automated protocol for mid-throughput soluble HLA immunopeptidomics

Joshua D. Ooi, Terry C.C. Lim Kam Sian, Isaac B. Woodhouse, Joel R. Steele, Pouya Faridi, Erwin Tanuwidjaya, Ralf B. Schittenhelm, Gabriel Gonçalves, Janet Chang
article en
1 citations

Abstract

Human leukocyte antigen (HLA) molecules are pivotal in guiding human adaptive immune responses through their presentation of peptide ligands, collectively known as the immunopeptidome. This process is central to the development of cancer immunotherapies, such as vaccines and T-cell therapies. Profiling the immunopeptidome from plasma and other biofluids has gained increasing traction, as it offers a minimally invasive approach for monitoring disease states and immune responses toward cancer therapy. Here we present the second iteration of SAPrIm, a refined immunopeptidomics tool optimized for soluble HLA analysis. It can process up to 12 samples per batch within a day. In this plasma-focused iteration, we identified approximately 1,200 to 4,000 immunopeptides from 100 µL to 1 mL of plasma, demonstrating high reproducibility across technical replicates, biological replicates, and inter-day analyses. This robust reproducibility highlights the method's strong potential for reliable relative quantification of immunopeptides in plasma-based studies. This workflow is positioned to advance the field of immunopeptidomics by enabling efficient plasma-based comparative analyses and mid-size cohort studies.

Frontiers in ImmunologyVol. 16
Discovery Institute (US), Hudson Institute of Medical Research (AU), Monash University (AU)
Openalex Percentile: Top 29%
vaccines and immunoinformatics approaches
0.81
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SAPrIm 2.0: a semi-automated protocol for mid-throughput soluble HLA immunopeptidomics — Joshua D. Ooi, Terry C.C. Lim Kam Sian, et al. · Frontiers in Immunology (2025) | TGRS Research Map | TGRS